Is this your brand? Sign in to claim ownership.
Sign in to claim this brandTRINITY STERILE, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 201 Kiley Dr, SALISBURY, MD, 21801
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000123297
- DUNS Number
- —
Catalogue (390)
Page 5 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trinity Sterile, Inc. | 81429 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5046 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6040 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5065 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81433 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5097 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 22101 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81248 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50142 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T98-384 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50562 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 6034 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-209 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85286UMT2 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81431 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85287SJ | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50329 | FDA UDI | N/A | Active |
| Trinity Sterile, Inc. | 6019 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5087 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5003 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7006 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 22001 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5038 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-123 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5002 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5078 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7038 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-268 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20313 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6032 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7014 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50106 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 7042 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81243 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5004 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50323 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50904 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50698 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81364 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-505 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50100 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T98-109 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 86123 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7093NSTRL | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85315 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5066 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 96-3615 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5044 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20107 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 7028 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (10)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 13, 2024 | Z-1012-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1016-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1015-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1013-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1014-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Jun 29, 2022 | Z-1551-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1548-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1550-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1549-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Feb 23, 2021 | Z-1468-2021 | — | terminated | Evidence of face masks or other material in the seal in several kits, causing improper seals and compromised sterility |